GLPBio

Deschloroclozapine dihydrochloride

Catalog No.: GC74124Purity:>98.00%
Deschloroclozapine dihydrochloride، مستقلب كلوزابين، هو مؤثر مسكاريني قوي DREADDs.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


Deschloroclozapine dihydrochloride
10mM (in 1mL DMSO)In Stock
$56.00
1
1mgIn Stock
$17.00
1
5mgIn Stock
$48.00
1
10mgIn Stock
$77.00
1
25mgIn Stock
$124.00
1
50mgIn Stock
$175.00
1
100mgIn Stock
$263.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
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الوصف (Description)

Deschloroclozapine dihydrochloride is a high-affinity, selective, and metabolically stable muscarinic DREADD agonist. Deschloroclozapine dihydrochloride can rapidly cross the blood-brain barrier and effectively activate both excitatory hM3Dq and inhibitory hM4Di DREADD receptors[1-2]. Deschloroclozapine dihydrochloride is primarily used in neuroscience for chemogenetic research to precisely modulate neuronal activity[3-4].

In vivo, In transgenic neuropathic pain model rats expressing hM3Dq, subcutaneous injection of Deschloroclozapine dihydrochloride (0.1mg/kg) for 120 minutes significantly increased serum OXT levels and rapidly raised the rats' mechanical pain threshold[5]. In transgenic mice expressing hM3Dq, intraperitoneal administration of Deschloroclozapine dihydrochloride (1mg/kg) for 5–10 minutes rapidly enhanced neuronal activity via hM3Dq, with an efficacy more than 2.5 times greater than that of Clozapine N-oxide (CNO; 100μg/kg), and brain concentrations of Deschloroclozapine dihydrochloride reached approximately 100 nM at 30 minutes[6].

References:
[1] Maggs JL, Williams D, Pirmohamed M, et al. The metabolic formation of reactive intermediates from clozapine, a drug associated with agranulocytosis in man. J Pharmacol Exp Ther. 1995 Dec;275(3):1463-75.
[2] Zhang S, Gumpper RH, Huang XP, et al. Molecular basis for selective activation of DREADD-based chemogenetics. Nature. 2022 Dec;612(7939):354-362.
[3] Nentwig TB, Obray JD, Vaughan DT, et al. Behavioral and slice electrophysiological assessment of DREADD ligand, Deschloroclozapine dihydrochloride (DCZ) in rats. Sci Rep. 2022 Apr 21;12(1):6595.
[4] Hu F, Morris PJ, Bonaventura J, et al. 18F-labeled radiotracers for in vivo imaging of DREADD with positron emission tomography. Eur J Med Chem. 2021 Mar 5;213:113047.
[5] Nagai Y, Miyakawa N, Takuwa H, et al. Deschloroclozapine dihydrochloride, a potent and selective chemogenetic actuator enables rapid neuronal and behavioral modulations in mice and monkeys. Nat Neurosci. 2020 Sep;23(9):1157-1167.
[6] Shimizu M, Yoshimura M, Baba K, et al. Deschloroclozapine dihydrochloride exhibits an exquisite agonistic effect at lower concentration compared to clozapine-N-oxide in hM3Dq expressing chemogenetically modified rats. Front Neurosci. 2023 Nov 30;17:1301515.

البروتوكول (Protocol)

Animal experiment [1]:

Animal models

OXT-hM3Dq-mCherry transgenic rats (adult male).

Preparation Method

Rats were subcutaneously (s.c.) administered a single dose of Deschloroclozapine dihydrochloride (0.1mg/kg). Serum oxytocin (OXT) concentrations were measured at 0, 10, 30, 60, 120, and 180 minutes post-injection. Brain neuronal activity (Fos expression) was assessed 120 minutes post-injection. In a neuropathic pain model (Seltzer model), behavioral tests (von Frey test, Rat Grimace Scale, hot plate test) were conducted at 0, 10, 30, 60, 120, and 180 minutes post-Deschloroclozapine dihydrochloride administration.

Dosage form

0.1mg/kg; s.c.; Single injection.

Applications

Deschloroclozapine dihydrochloride administration induced a rapid and robust increase in serum OXT levels, Deschloroclozapine dihydrochloride significantly enhanced neuronal activation (Fos expression) in brain regions including the SON, PVN, and PAG comparable to a 10-fold higher dose of CNO, and produced rapid analgesic effects in a neuropathic pain model (significantly increasing mechanical nociceptive threshold and reducing pain scores within 10 minutes).

References:
[1] Shimizu M, Yoshimura M, Baba K, et al. Deschloroclozapine dihydrochloride exhibits an exquisite agonistic effect at lower concentration compared to clozapine-N-oxide in hM3Dq expressing chemogenetically modified rats. Front Neurosci. 2023 Nov 30;17:1301515.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

الصيغة الجزيئية
C18H22Cl2N4
الوزن الجزيئي
365.3
الذوبانية
H2O : 100 mg/mL (273.75 mM; Need ultrasonic); DMSO : 80 mg/mL (219.00 mM; ultrasonic and adjust pH to 7 with 1 M NaOH)
التخزين
-20°C, sealed storage, away from moisture
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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